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1,291 results for “gap”
Simulation data for the article ,,Filling the gap with long n-alkanes: incorporation of C20 and C30 into phospholipid membranes" - Set3
<p>First set of simulation trajectories and input files for the manuscript ,,Filling the gap with long n-alkanes: incorporation of C20 and C30 into phospholipid membranes".</p> <p>System: DPPC + n-triacontane (CHARMM36); 288 DPPC, 19 water molecules per lipid, 343K</p> <p>Numbers of n-triacontane molecules are given in the file names.</p> <p>Simulations consisted of three 100ns runs, an .xtc trajectory is only included for the final run. Trajectories were created with -dt 10(ps) and -pbc nojump, as used for analysis in the manuscript. Solvent molecules were removed from the trajectories for file size reduction.</p>
Simulation data for the article ,,Filling the gap with long n-alkanes: incorporation of C20 and C30 into phospholipid membranes" - Set1
<p>First set of simulation trajectories and input files for the manuscript ,,Filling the gap with long n-alkanes: incorporation of C20 and C30 into phospholipid membranes".</p> <p>Systems: DPPC + n-decane (CHARMM36); 72 DPPC, 7 water molecules per lipid, 333K unless otherwise noted in the file names.</p> <p>Numbers of n-decane molecules are given in the file names.</p> <p>Simulations consisted of three 100ns runs, an .xtc trajectory is only included for the final run. Trajectories were created with -dt 10(ps) and -pbc nojump, as used for analysis in the manuscript. Solvent molecules were removed from the trajectories for file size reduction.</p>
Simulation data for the article ,,Filling the gap with long n-alkanes: incorporation of C20 and C30 into phospholipid membranes" - Set2
<p>First set of simulation trajectories and input files for the manuscript ,,Filling the gap with long n-alkanes: incorporation of C20 and C30 into phospholipid membranes" (submitted to Langmuir, under peer-review).</p> <p>System: DPPC + n-eicosane (CHARMM36); 72 DPPC, 18 water molecules per lipid, 333K, unless otherwise noted in the file name.</p> <p>Numbers of n-eicosane molecules are given in the file names.</p> <p>Simulations consisted of three 100ns runs, an .xtc trajectory is only included for the final run. Trajectories were created with -dt 10(ps) and -pbc nojump, as used for analysis in the manuscript. Solvent molecules were removed from the trajectories for file size reduction.</p>
Distribution. Two geographically disjunct ranges, including arid parts of extreme SW Angola, W Namibia, and W South Africa S to Western Cape Province, and N Mozambique, E & S Zimbabwe, extreme E Botswana, and N South Africa; an 800km-gap separates the two parts of the species' range between Augrabies Falls on the Orange River in W South Africa and the Magaliesberg of North West and Gauteng provinces in N South Africa. in Molossidae
Distribution. Two geographically disjunct ranges, including arid parts of extreme SW Angola, W Namibia, and W South Africa S to Western Cape Province, and N Mozambique, E & S Zimbabwe, extreme E Botswana, and N South Africa; an 800km-gap separates the two parts of the species' range between Augrabies Falls on the Orange River in W South Africa and the Magaliesberg of North West and Gauteng provinces in N South Africa.
Distribution. Poorly known, but it appears to be restricted to cooler waters of the Southern Hemisphere between 32° S and the Antarctic convergence; it has been recorded stranding in New Zealand, Australia, Tristan da Cunha, and Tierra del Fuego. Its distribution may be circumpolar, but it is also possible that there is a gap in its distribution between the Chatham Is and South America. in Ziphiidae
Distribution. Poorly known, but it appears to be restricted to cooler waters of the Southern Hemisphere between 32° S and the Antarctic convergence; it has been recorded stranding in New Zealand, Australia, Tristan da Cunha, and Tierra del Fuego. Its distribution may be circumpolar, but it is also possible that there is a gap in its distribution between the Chatham Is and South America.
Enhancing georeferenced biodiversity inventories: automated information extraction from literature records reveal the gaps
<p>Data and code supplement to our article revised submission to PeerJ.</p> <p> </p> <p>The file is compressed using standard zip. The uncompressed size is about 50 GB. There is a readme.md in the archive, which explains the structure of the contents.</p> <p> </p> <p>Abstract:</p> <p>We use natural language processing (NLP) to retrieve location data for cheilostome bryozoan species (text-mined occurrences [TMO]) in an automated procedure. We compare these results with data combined from two major public databases (DB): the Ocean Biogeographic Information System (OBIS), and the Global Biodiversity Information Facility (GBIF). Using DB and TMO data separately and in combination, we present latitudinal species richness curves using standard estimators (Chao2 and the Jackknife) and range-through approaches. Our combined DB and TMO species richness curves quantitatively document a bimodal global latitudinal diversity gradient for extant cheilostomes for the first time, with peaks in the temperate zones. 79% of the georeferenced species we retrieved from TMO (N = 1408) and DB (N = 4549) are non-overlapping. Despite clear indications that global location data compiled for cheilostomes should be improved with concerted effort, our study supports the view that many marine latitudinal species richness patterns deviate from the canonical latitudinal diversity gradient (LDG). Moreover, combining online biodiversity databases with automated information retrieval from the published literature is a promising avenue for expanding taxon-location datasets.</p>
Distribution. Patchily in forests not more than 350 km inland from the coast in S Nigeria (W limit in forests near Dahomey Gap), W Cameroon, W Equatorial Guinea, W Gabon, and SW of the Republic of Congo (as far S as Conkouati-Douli National Park); there have been unconfirmed reports of its occurrence in Benin, butif it ever did occur there, it may now be extirpated, as was a former population near the Benue River in Nigeria. in Cercopithecidae
Distribution. Patchily in forests not more than 350 km inland from the coast in S Nigeria (W limit in forests near Dahomey Gap), W Cameroon, W Equatorial Guinea, W Gabon, and SW of the Republic of Congo (as far S as Conkouati-Douli National Park); there have been unconfirmed reports of its occurrence in Benin, butif it ever did occur there, it may now be extirpated, as was a former population near the Benue River in Nigeria.
Distribution. NE India (S of the Brahmaputra River in the states of Assam, E Arunachal Pradesh, Manipur, Meghalaya, Mizoram, Nagaland & Tripura), extending SE through E Bangladesh and Myanmar (including the Mergui Archipelago), S China (SW Yunnan Province), Thailand, Laos, Vietnam, and Cambodia; S to the Surat Thani/Krabi depression in peninsular Thailand (8-9° N). The lack of records in C and NE Myanmar between 20° N and 25° N suggests that this may be a natural gap in the distribution of the Northern Pig-tailed Macaque. in Cercopithecidae
Distribution. NE India (S of the Brahmaputra River in the states of Assam, E Arunachal Pradesh, Manipur, Meghalaya, Mizoram, Nagaland & Tripura), extending SE through E Bangladesh and Myanmar (including the Mergui Archipelago), S China (SW Yunnan Province), Thailand, Laos, Vietnam, and Cambodia; S to the Surat Thani/Krabi depression in peninsular Thailand (8-9° N). The lack of records in C and NE Myanmar between 20° N and 25° N suggests that this may be a natural gap in the distribution of the Northern Pig-tailed Macaque.
Distribution. Dahomey Gap in Togo, Benin, and W Nigeria; it is presumed to occur in extreme E Ghana E of Volta River. in Muridae
Distribution. Dahomey Gap in Togo, Benin, and W Nigeria; it is presumed to occur in extreme E Ghana E of Volta River.
On following pages: 578. African Smoky Mouse (Heimyscus fumosus); 579. Baer's Wood Mouse (Hylomyscus baer); 580. Mount Oku Wood Mouse (Hylomyscus grandis); 581. Dahomey Gap Wood Mouse (Hylomyscus pamfi), 582. West African Wood Mouse (Hylomyscus simus); 583. Beaded Wood Mouse (Hylomyscus aeta); 584. Allen's Wood Mouse (Hylomyscus alleni); 585. Ansell's Wood Mouse (Hylomyscus ansell); 586. Lesser Wood Mouse (Hylomyscus parvus); 587. Walter Verheyen's Wood Mouse (Hylomyscus walterverheyeni); 588. Stella Wood Mouse (Hylomyscus stella); 589. Albertine Rift Wood Mouse (Hylomyscus vulcanorum); 590. Eastern Arc Wood Mouse (Hylomyscus arcimontensis); 591. Montane Wood Mouse (Hylomyscus denniae); 592. Mount Kenya Wood Mouse (Hylomyscus endorobae); 593. Tanzanian Wood Mouse (Hylomyscus kaimosae), 594. Kerbis-Peterhans''s Wood Mouse (Hylomyscus kerbispeterhansi); 595. Angolan Wood Mouse (Hylomyscus carillus); 596. Heinrich's Wood Mouse (Hylomyscus heinrichorum); 597. Awash Multimammate Mouse (Mastomys awashensis), 598. Natal Multimammate Mouse (Mastomys natalensis); 599. Reddish-white Multimammate Mouse (Mastomys erythroleucus); 600. Hubert's Multimammate Mouse (Mastomys hubert)); 601. Kollmannsperger's Multimammate Mouse (Mastomys kollmannspergeri); 602. Dwarf Multimammate Mouse (Mastomys pernanus); 603. Southern African Multimammate Mouse (Mastomys coucha); 604. Shortridge's Multimammate Mouse (Mastomys shortridge). in Muridae
On following pages: 578. African Smoky Mouse (Heimyscus fumosus); 579. Baer's Wood Mouse (Hylomyscus baer); 580. Mount Oku Wood Mouse (Hylomyscus grandis); 581. Dahomey Gap Wood Mouse (Hylomyscus pamfi), 582. West African Wood Mouse (Hylomyscus simus); 583. Beaded Wood Mouse (Hylomyscus aeta); 584. Allen's Wood Mouse (Hylomyscus alleni); 585. Ansell's Wood Mouse (Hylomyscus ansell); 586. Lesser Wood Mouse (Hylomyscus parvus); 587. Walter Verheyen's Wood Mouse (Hylomyscus walterverheyeni); 588. Stella Wood Mouse (Hylomyscus stella); 589. Albertine Rift Wood Mouse (Hylomyscus vulcanorum); 590. Eastern Arc Wood Mouse (Hylomyscus arcimontensis); 591. Montane Wood Mouse (Hylomyscus denniae); 592. Mount Kenya Wood Mouse (Hylomyscus endorobae); 593. Tanzanian Wood Mouse (Hylomyscus kaimosae), 594. Kerbis-Peterhans''s Wood Mouse (Hylomyscus kerbispeterhansi); 595. Angolan Wood Mouse (Hylomyscus carillus); 596. Heinrich's Wood Mouse (Hylomyscus heinrichorum); 597. Awash Multimammate Mouse (Mastomys awashensis), 598. Natal Multimammate Mouse (Mastomys natalensis); 599. Reddish-white Multimammate Mouse (Mastomys erythroleucus); 600. Hubert's Multimammate Mouse (Mastomys hubert)); 601. Kollmannsperger's Multimammate Mouse (Mastomys kollmannspergeri); 602. Dwarf Multimammate Mouse (Mastomys pernanus); 603. Southern African Multimammate Mouse (Mastomys coucha); 604. Shortridge's Multimammate Mouse (Mastomys shortridge).
Distribution. Upper Guinea Forest of W Africa W of Dahomey Gap, extending from Sierra Leone Eto Ghana. in Muridae
Distribution. Upper Guinea Forest of W Africa W of Dahomey Gap, extending from Sierra Leone Eto Ghana.
Distribution. Widely distributed in tropical Africa from Dahomey Gap E to Ethiopia and S to N Angola, S DR Congo, and SW Tanzania. in Muridae
Distribution. Widely distributed in tropical Africa from Dahomey Gap E to Ethiopia and S to N Angola, S DR Congo, and SW Tanzania.
Distribution. Occurs widely in W Africa in forested habitats from E Sierra Leone E to SW Nigeria (W of Niger River), but absent from the Dahomey Gap (SE Ghana, Togo, and Benin). in Muridae
Distribution. Occurs widely in W Africa in forested habitats from E Sierra Leone E to SW Nigeria (W of Niger River), but absent from the Dahomey Gap (SE Ghana, Togo, and Benin).
Distribution. Hinterland of Gulf of Papua, from Lake Murray and upper Fly River catchment E to Astrolabe Range and Kokoda Gap area of Owen Stanley Range, New Guinea. in Muridae
Distribution. Hinterland of Gulf of Papua, from Lake Murray and upper Fly River catchment E to Astrolabe Range and Kokoda Gap area of Owen Stanley Range, New Guinea.
Distribution. Papuan Peninsula of New Guinea, including Astrolabe, Owen Stanley (W to Mt Albert Edward and Kokoda Gap), and Maneau ranges (Mt Simpson, Mt Mura, Mt Suckling, and Mt Dayman). in Muridae
Distribution. Papuan Peninsula of New Guinea, including Astrolabe, Owen Stanley (W to Mt Albert Edward and Kokoda Gap), and Maneau ranges (Mt Simpson, Mt Mura, Mt Suckling, and Mt Dayman).
Code and Data for "Bridging Gaps in the Climate Observation Network"
<p>The code and data used in the paper "Bridging Gaps in the Climate Observation Network: A Physics-based Nonlinear Dynamical Interpolation of Lagrangian Ice Floe Measurements via Data-Driven Stochastic Model"</p>
The Early Functional Abilities-revised may bridge the gap between the disorder of consciousness and the functional independence scales: evidence from Rasch analysis
<p>Raw data associated with the scientific publication “The Early Functional Abilities-revised may bridge the gap between the disorder of consciousness and the functional independence scales: evidence from Rasch analysis”</p>
Figure 3 in Ants (Hymenoptera: Formicidae) from Miocene Ethiopian amber: filling gaps in the geological record of African terrestrial biota
Figure 3. Technomyrmex svojtkai sp. nov., photomicrographs of paratype workers and additional, partial worker, specimen MAIG 6020. A, paratype 1, ventral view. B, paratype 2, dorsal view. C, paratype 2, left lateral view, anterior-oblique orientation. D, non-type, partially preserved worker, right lateral view. Scale bars: 0.25 mm.
Figure 2 in Ants (Hymenoptera: Formicidae) from Miocene Ethiopian amber: filling gaps in the geological record of African terrestrial biota
Figure 2. Technomyrmex svojtkai sp. nov. Phase contrast X-ray synchrotron microtomography of holotype worker NHMW-N6976, with indication of measurements as reported in Material and methods. A, lateral view of body with legs and antennae virtually removed, and with petiole and gaster virtually uncurled to approximate the life position. The left lateral side of the head and mesosoma being crushed, the figure shows them from the horizontally flipped right side in standard left profile view. B, reconstruction in dorsal view, without legs and antennae, and with gaster largely concealing the petiole as in approximate life position. C, head in full-face view. D, head without antennae in full-face view. E, mandibles in dorsal view. F, petiole in dorsal view, with articulation with gaster as preserved. F, gaster in ventral view, with articulation with petiole as preserved, showing the first gastral tergite concavity for accommodation of petiole. Abbreviations: AIII–AVII, abdominal segments III to VII. Scale bars: 0.5 mm, except 0.2 mm for E.
Figure 1 in Ants (Hymenoptera: Formicidae) from Miocene Ethiopian amber: filling gaps in the geological record of African terrestrial biota
Figure 1. Technomyrmex svojtkai sp. nov., holotype worker NHMW-N6976. A, photomicrograph in right lateral view, with tip of gaster curled toward the mouthparts. B, 3D model in nearly the same position, imaged by synchrotron microtomography. C–E, 3D model of body with antennae and legs virtually removed: C, anterior (frontal) view; D, left lateral view; E, posterior (dorsal) view. Scale bar: 0.5 mm. Animated versions of this are available in Supporting Information online (Figs S1, S2).
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.